A comparative study of transfusion-acquired human immunodeficiency virus-infected children with and without

D Gleason-Morgan1, J A Church, L A Ross

  • 1Division of Allergy-Clinical Immunology, Childrens Hospital Los Angeles 90027.

Insights

Disseminated Mycobacterium avium complex (DMAC) in children with advanced HIV disease is associated with significantly lower survival rates. Early identification requires a high index of suspicion due to nonspecific clinical and laboratory features.

Area of Science:

  • Pediatric Infectious Diseases
  • Immunology
  • HIV/AIDS Research

Background:

  • Disseminated Mycobacterium avium complex (DMAC) is a significant opportunistic infection in individuals with advanced human immunodeficiency virus (HIV) disease.
  • Understanding the specific features of DMAC in pediatric populations is crucial for timely diagnosis and management.

Purpose of the Study:

  • To identify the clinical and laboratory features distinguishing disseminated Mycobacterium avium complex (DMAC) in human immunodeficiency virus (HIV)-infected children.
  • To assess the impact of DMAC on survival in this vulnerable pediatric cohort.

Main Methods:

  • Retrospective medical record review of 31 long-term survivors with transfusion-acquired HIV.
  • Comparison of laboratory markers (CD4+ T cell counts, HIV p24 antigen, aspartate aminotransferase) and clinical signs (fever, abdominal pain) between DMAC-positive and DMAC-negative patients.

Main Results:

  • Nine patients developed DMAC, diagnosed between 51-132 months of age.
  • DMAC-positive patients exhibited significantly lower CD4+ T cell counts and higher HIV p24 antigen levels.
  • Fever and abdominal pain were more frequent in DMAC-positive children; overall survival was lower (33% vs. 73%).

Conclusions:

  • DMAC occurs in profoundly immunocompromised children with advanced HIV disease, significantly impacting survival.
  • Clinical and laboratory features of DMAC are nonspecific, necessitating a high index of suspicion in patients with severely reduced CD4+ T cells.